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使用全息光镊在胚胎干细胞聚集体中创建生化梯度以实现基因表达的局部诱导。

Localized Induction of Gene Expression in Embryonic Stem Cell Aggregates Using Holographic Optical Tweezers to Create Biochemical Gradients.

作者信息

Kirkham Glen R, Ware James, Upton Thomas, Allen Stephanie, Shakesheff Kevin M, Buttery Lee Dk

机构信息

College of Science and Technology, Nottingham Trent University, Nottingham, NG11 8NS UK.

School of Pharmacy, University of Nottingham, Nottingham, NG7 2RD UK.

出版信息

Regen Eng Transl Med. 2020;6(3):251-261. doi: 10.1007/s40883-019-00114-5. Epub 2019 Aug 26.

Abstract

Three-dimensional (3D) cell models that mimic the structure and function of native tissues are enabling more detailed study of physiological and pathological mechanisms in vitro. We have previously demonstrated the ability to build and manipulate 3D multicellular microscopic structures using holographic optical tweezers (HOTs). Here, we show the construction of a precisely patterned 3D microenvironment and biochemical gradient model consisting of mouse embryoid bodies (mEBs) and polymer microparticles loaded with retinoic acid (RA), embedded in a hydrogel. We demonstrate discrete, zonal expression of the RA-inducible protein Stra8 within mEBs in response to release of RA from polymer microparticles, corresponding directly to the defined 3D positioning of the microparticles using HOTs. These results demonstrate the ability of this technology to create chemical microgradients at definable length scales and to elicit, with fidelity and precision, specific biological responses. This technique can be used in the study of in vitro microenvironments to enable new insights on 3D cell models, their cellular assembly, and the delivery of drug or biochemical molecules for engineering and interrogation of functional and morphogenic responses Graphical abstract.

摘要

模拟天然组织结构和功能的三维(3D)细胞模型能够在体外更详细地研究生理和病理机制。我们之前已经证明了使用全息光镊(HOTs)构建和操纵3D多细胞微观结构的能力。在此,我们展示了一种精确图案化的3D微环境和生化梯度模型的构建,该模型由小鼠胚胎体(mEBs)和负载视黄酸(RA)的聚合物微粒组成,嵌入水凝胶中。我们证明了响应于聚合物微粒释放的RA,mEBs内RA诱导蛋白Stra8的离散、区域表达,这直接对应于使用HOTs对微粒进行的定义3D定位。这些结果证明了该技术在可定义的长度尺度上创建化学微梯度以及以保真度和精度引发特定生物学反应的能力。该技术可用于体外微环境研究,以获得关于3D细胞模型、其细胞组装以及用于工程和询问功能及形态发生反应的药物或生化分子递送的新见解 图形摘要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b611/7505830/753e92ec6249/40883_2019_114_Figa_HTML.jpg

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